重组酶聚合酶扩增
微流控
清脆的
注意事项
检出限
检测点注意事项
纳米技术
生物传感器
计算生物学
材料科学
医学
计算机科学
生物
聚合酶链反应
病理
化学
遗传学
色谱法
基因
作者
Shixian Liu,Yu Tian,Li-Bing Song,Kourosh Kalantar‐zadeh,Guozhen Liu
出处
期刊:ACS Sensors
[American Chemical Society]
日期:2025-05-19
卷期号:10 (6): 4569-4579
标识
DOI:10.1021/acssensors.5c00863
摘要
Highly sensitive point-of-care early screening for high-risk human papillomavirus (HPV) infections is urgently needed, particularly in resource-limited settings. Nucleic acid amplification methods, especially CRISPR/Cas-based biosensors, have emerged as promising tools for sensitive HPV detection; however, current approaches typically rely on tedious tube-based formats coupled with lateral flow assays for signal readout in point-of-care testing (POCT). Here, we developed customized microfluidic paper-based analytical devices (μPADs) with valves that seamlessly integrated recombinase polymerase amplification (RPA) with CRISPR/Cas12a biosensing (RPA-CRISPR/Cas12a) on the filter paper substrate. This innovation achieved sensitive and cost-effective high-risk HPV detection in POCT. The RPA-CRISPR/Cas12a system with a linear reporter on μPADs, enabled fluorescence detection of the E7 gene, achieving a sensitivity of 1 pM at approximately 1 h. The sensitivity was further enhanced by introducing a circular reporter into the fluorescence-based RPA-CRISPR/Cas12a system on μPADs, enabling detection of the E7 gene with a detection limit of 1 fM and an assay time of 35 min. The system was validated using 50 cervical swab clinical samples, demonstrating 95% sensitivity and 100% specificity when compared to qPCR. This sample-to-answer detection platform holds significant promise for early screening of high-risk HPV infections in point-of-care scenarios.
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